Electrodes for abdominal fetal electrocardiogram detection

ABSTRACT

The invention provides systems and methods for monitoring the wellbeing of a fetus by the non-invasive detection and analysis of fetal cardiac electrical activity data.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation application of U.S. patentapplication Ser. No. 15/071,956, filed Mar. 16, 2016, which claimspriority to U.S. Provisional Patent Application No. 62/133,485, filed onMar. 16, 2015, and U.S. patent application Ser. No. 14/921,489, filed onOct. 23, 2015, the entire contents of which are incorporated byreference in their entirety.

FIELD OF THE INVENTION

The invention relates generally to electrodes suitable for use in fetalheart rate monitoring systems.

BACKGROUND

Monitoring fetal cardiac electrical activity can be useful to determineof the health of a fetus during pregnancy.

SUMMARY

In one embodiment, the present invention provides an electrodeconfigured to detect fetal electrocardiogram signals, comprising:

-   -   a) a cutaneous contact for sensing fetal electrocardiogram        signals from a pregnant human subject;    -   b) a connector in electrical contact with the cutaneous contact        for connection to a lead wire; and    -   c) a substructure for attachment to a human pregnant subject,        -   wherein, the cutaneous contact is configured on the            substructure to allow a surface of the cutaneous contact to            be in electrical communication with the skin of the pregnant            human subject.

In one embodiment, the cutaneous contact is configured to haveskin-electrode impedance of greater than 150 kΩ.

In one embodiment, the cutaneous contact is configured to haveskin-electrode impedance of less than 150 kΩ.

In one embodiment, the cutaneous contact is configured to haveskin-electrode impedance of between 5 to 150 kΩ.

In one embodiment, the cutaneous contact is attached to an elastomericstructure that is configured to deform when placed on the abdomen of thepregnant human subject to create a skin-electrode impedance of less than150 kΩ.

In one embodiment, the cutaneous contact is attached to an elastomericstructure that is configured to deform when placed on the abdomen of thepregnant human subject to create a skin-electrode impedance of between 5to 150 kΩ.

In one embodiment, the cutaneous contact is configured to have a surfaceresistance of less than 1 Ω/square.

In one embodiment, the cutaneous contact is configured to have a surfaceresistance between 0.01 and 1 Ω/square.

In one embodiment, the signal to noise ratio of the fetalelectrocardiogram signals is between −20 dB and 50 dB.

In one embodiment, the signal to noise ratio of the fetalelectrocardiogram signals is between 0 dB and 50 dB.

In one embodiment, the signal to noise ratio of the fetalelectrocardiogram signals is less than 50 dB.

In one embodiment, the cutaneous contact is an electrically conductivefabric.

In one embodiment, the electrically conductive fabric has askin-electrode impedance of less than 150 kΩ.

In one embodiment, the electrically conductive fabric has askin-electrode impedance of between 5 to 150 kΩ.

In one embodiment, the surface of the electrically conductive fabricthat forms the cutaneous contact is configured to have a surfaceresistance of less than 1 Ω/square.

In one embodiment, the present invention provides a garment, comprising:

at least one pair of electrodes,

-   -   wherein the at least one pair of electrodes are configured, when        the garment is worn by the pregnant human subject, such that the        individual electrodes of the at least one electrode pair        encircle the uterus of the pregnant human subject, and    -   wherein the individual electrodes of the at least one electrode        pair comprise:        -   a) a cutaneous contact for sensing fetal electrocardiogram            signals from a pregnant human subject;        -   b) a connector in electrical contact with the cutaneous            contact for connection to a lead wire; and        -   c) a substructure for attachment to a human pregnant            subject,            -   wherein, the cutaneous contact is configured on the                substructure to allow a surface of the cutaneous contact                to be in electrical communication with the skin of the                pregnant human subject;    -   wherein cardiac electrical activity data is recorded from the at        least one sensor pair.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows an electrode according to some embodiments of the presentinvention.

FIG. 2 shows an electrode according to some embodiments of the presentinvention.

FIG. 3 shows an electrode according to some embodiments of the presentinvention.

FIG. 4 shows an electrode according to some embodiments of the presentinvention.

FIG. 5 shows a micrograph of electrically conductive fabric suitable asa cutaneous contact according to some embodiments of the presentinvention.

FIG. 6 shows a micrograph of electrically conductive fabric suitable asa cutaneous contact according to some embodiments of the presentinvention.

FIG. 7 shows a micrograph of electrically conductive fabric suitable asa cutaneous contact according to some embodiments of the presentinvention.

FIG. 8 shows a micrograph of electrically conductive fabric suitable asa cutaneous contact according to some embodiments of the presentinvention.

FIG. 9 shows a micrograph of electrically conductive fabric suitable asa cutaneous contact according to some embodiments of the presentinvention.

FIG. 10 shows a micrograph of electrically conductive fabric suitable asa cutaneous contact according to some embodiments of the presentinvention.

FIGS. 11A-B show the positions of the ECG sensor pairs on the abdomen ofa pregnant woman according to some embodiments of the present invention.Panel a) shows a front view. Panel b) shows a side view.

FIG. 12 shows a representation of a system suitable for use in fetalheart rate monitoring systems according to some embodiments of thepresent invention.

FIG. 13 shows a garment according to some embodiments of the presentinvention.

FIG. 14, panels a-c show recorded ECG signals data using electrodeserial nos. 3-5 respectively.

FIG. 15, panels a-d, show the recorded ECG signals data using electrodeserial nos. 3-5, and a control wet gel ECG electrode (GE Healthcare),respectively at 25 weeks from a pregnant human subject.

FIG. 16, panels a-d, show the recorded ECG signals data using electrodeserial nos. 3-5, and a control wet gel ECG electrode (GE), respectivelyat 25 weeks from a pregnant human subject.

FIG. 17 shows an experimental set up to determine surface resistivityand resistance of an electrically conductive fabric according to someembodiments of the present invention.

FIG. 18 shows an experimental set up to determine BTFT of anelectrically conductive fabric according to some embodiments of thepresent invention.

FIG. 19 shows a diagram if a skin-electrode interface equivalent circuitaccording to some embodiments of the present invention.

FIG. 20 shows a representation of a test electrode configuration.

DETAILED DESCRIPTION

For clarity of disclosure, and not by way of limitation, the detaileddescription of the invention is divided into the following subsectionsthat describe or illustrate certain features, embodiments orapplications of the present invention.

As used herein the term “contact region” encompasses the contact areabetween the skin of a pregnant human subject and cutaneous contact i.e.the surface area through which current flow can pass between the skin ofthe pregnant human subject and the cutaneous contact.

In some embodiments, the present invention provides a system fordetecting, recording and analyzing cardiac electrical activity data froma pregnant human subject. In some embodiments, a plurality of electrodesconfigured to detect fetal electrocardiogram signals is used to recordthe cardiac activity data. In some embodiments, a plurality ofelectrodes configured to detect fetal electrocardiogram signals and aplurality of acoustic sensors are used to record the cardiac activitydata.

In some embodiments, a plurality of electrodes configured to detectfetal electrocardiogram signals are attached to the abdomen of thepregnant human subject. In some embodiments, the plurality of electrodesconfigured to detect fetal electrocardiogram signals are directlyattached. In some embodiments, the plurality of electrodes configured todetect fetal electrocardiogram signals are incorporated into an article,such as, for example, a belt, a patch, and the like, and the article isworn by, or placed on, the pregnant human subject.

In some embodiments, the present invention provides an electrodeconfigured to detect fetal electrocardiogram signals, comprising:

-   -   a) a cutaneous contact for sensing fetal electrocardiogram        signals from a pregnant human subject;    -   b) a connector in electrical contact with the cutaneous contact        for connection to a lead wire; and    -   c) a substructure for attachment to a human pregnant subject        -   wherein, the cutaneous contact is configured on the            substructure to allow a surface of the cutaneous contact to            be in electrical communication with the skin of the pregnant            human subject.

Without intending to be limited to any particular theory, in someembodiments, the three-dimensional shape of the electrode affects theperformance. For example, a curved profile without sharp angles islikely to prevent abrupt changes in the electrical field generated bythe cutaneous contact, or flow of current from the cutaneous contact tothe lead wire.

FIG. 1 shows a circular electrode according to some embodiments of thepresent invention. In the embodiment shown in FIG. 1, the electrode, asshown along the section A-A, comprises an electrically conductive fabric(5) attached over an elastomeric dome shaped circular structure (6),which is, in turn, attached to a circular foam backing (7). The foambacking is attached to a printed circuit board (8), which has oneelectrical connection (9) that outputs the sensed fetalelectrocardiogram signals, and at least one electrical connection (10)that connects the electrically conductive fabric to the printed circuitboard (8).

In some embodiments, the printed circuit board is configured tointerface the cutaneous contact with the lead wire. Alternatively, insome embodiments, the printed circuit board is further configured toperform additional functions, such as, for example, signal filtering, orpre-amplification.

FIG. 2 shows an electrode according to some embodiments of the presentinvention. In the embodiment shown, the electrode consists of ateardrop-shaped electrically conductive fabric, with a flat portion thatterminates at one end with a connection to a printed circuit board, anda dome-shaped structure that forms a skin contact at the opposite end.In the embodiment shown, only the dome-shaped structure would be exposedand touch the skin of the pregnant human subject.

FIGS. 3 and 4 show alternate embodiments of electrodes according to thepresent invention comprising a planar cutaneous contact.

In the embodiment shown in FIG. 1, the elastomeric dome shaped circularstructure is configured to maximize contact between the cutaneouscontact and the skin of the pregnant human subject under a all possibleattachment angles.

In the embodiment shown in FIG. 1, the elastomeric dome shaped circularstructure is configured to generate a profile without sharp angles whichare likely to affect performance of the electrode.

In some embodiments, the elastomeric dome shaped circular structure hasa diameter ranging from 20 to 50 mm. In some embodiments, theelastomeric dome shaped circular structure has a diameter of 20 mm. Insome embodiments, the elastomeric dome shaped circular structure has adiameter of 25 mm. In some embodiments, the elastomeric dome shapedcircular structure has a diameter of 30 mm. In some embodiments, theelastomeric dome shaped circular structure has a diameter of 35 mm. Insome embodiments, the elastomeric dome shaped circular structure has adiameter of 40 mm. In some embodiments, the elastomeric dome shapedcircular structure has a diameter of 45 mm. In some embodiments, theelastomeric dome shaped circular structure has a diameter of 50 mm.

In some embodiments, the elastomeric dome shaped circular structure hasan un-deformed height (i.e. a height before pressure is applied) rangingfrom 5 to 15 mm. In some embodiments, the elastomeric dome shapedcircular structure has an un-deformed height of 5 mm. In someembodiments, the elastomeric dome shaped circular structure has anun-deformed height of 10 mm. In some embodiments, the elastomeric domeshaped circular structure has an un-deformed height of 15 mm.

In some embodiments, the circular foam backing has a thickness rangingfrom 0.3 to 5 mm. In some embodiments, the circular foam backing has athickness of 0.3 mm. In some embodiments, the circular foam backing hasa thickness of 0.5 mm. In some embodiments, the circular foam backinghas a thickness of 1 mm. In some embodiments, the circular foam backinghas a thickness of 1.5 mm. In some embodiments, the circular foambacking has a thickness of 2 mm. In some embodiments, the circular foambacking has a thickness of 2.5 mm. In some embodiments, the circularfoam backing has a thickness of 3 mm. In some embodiments, the circularfoam backing has a thickness of 3.5 mm. In some embodiments, thecircular foam backing has a thickness of 4 mm. In some embodiments, thecircular foam backing has a thickness of 4.5 mm. In some embodiments,the circular foam backing has a thickness of 5 mm.

In the embodiment shown in FIG. 2, the elastomeric dome shaped circularstructure is configured to generate a profile without sharp angles whichare likely affect performance of the electrode. In some embodiments, theelastomeric dome shaped circular structure has a diameter ranging from15 to 38 mm. In some embodiments, the elastomeric dome shaped circularstructure has a diameter of 15 mm. In some embodiments, the elastomericdome shaped circular structure has a diameter of 20 mm. In someembodiments, the elastomeric dome shaped circular structure has adiameter of 25 mm. In some embodiments, the elastomeric dome shapedcircular structure has a diameter of 30 mm. In some embodiments, theelastomeric dome shaped circular structure has a diameter of 35 mm. Insome embodiments, the elastomeric dome shaped circular structure has adiameter of 38 mm.

In some embodiments, the elastomeric dome shaped circular structure hasan un-deformed height (i.e. a height before pressure is applied) rangingfrom 5 to 15 mm. In some embodiments, the elastomeric dome shapedcircular structure has an un-deformed height of 5 mm. In someembodiments, the elastomeric dome shaped circular structure has anun-deformed height of 10 mm. In some embodiments, the elastomeric domeshaped circular structure has an un-deformed height of 15 mm.

Without intending to be limited to any particular theory, theskin-electrode impedance varies with the pressure at which the electrodecontacts the skin of the pregnant human subject. In some embodiments,the skin-electrode impedance decreases as the pressure at which theelectrode contacts the skin of the pregnant human subject increases.

In some embodiments, the elastomeric dome is configured to deform whenplaced on the abdomen of the pregnant human subject and pressure isapplied to the electrode. In some embodiments, the elastomeric dome isconfigured to deform when placed on the abdomen of the pregnant humansubject and pressure applied to create a skin-electrode impedancesuitable for sensing fetal electrocardiogram signals from a pregnanthuman subject.

In some embodiments, the deformation of the elastomeric dome increasesthe surface area of the cutaneous contact that contacts the skin of thepregnant human subject. In some embodiments, 100% of the surface area ofthe cutaneous contact contacts the skin of the pregnant human subject.In an alternate embodiment, 90% of the surface area of the cutaneouscontact contacts the skin of the pregnant human subject. In an alternateembodiment, 80% of the surface area of the cutaneous contact contactsthe skin of the pregnant human subject. In an alternate embodiment, 70%of the surface area of the cutaneous contact contacts the skin of thepregnant human subject. In an alternate embodiment, 60% of the surfacearea of the cutaneous contact contacts the skin of the pregnant humansubject. In an alternate embodiment, 50% of the surface area of thecutaneous contact contacts the skin of the pregnant human subject. In analternate embodiment, 40% of the surface area of the cutaneous contactcontacts the skin of the pregnant human subject. In an alternateembodiment, 30% of the surface area of the cutaneous contact contactsthe skin of the pregnant human subject. In an alternate embodiment, 20%of the surface area of the cutaneous contact contacts the skin of thepregnant human subject. In an alternate embodiment, 10% of the surfacearea of the cutaneous contact contacts the skin of the pregnant humansubject. In an alternate embodiment, 75% of the surface area of thecutaneous contact contacts the skin of the pregnant human subject.

In some embodiments, the pressure applied is equivalent to a massranging between 0.2 kg to 5 kg. In some embodiments, the pressureapplied is equivalent to a mass of 0.2 kg. In some embodiments, thepressure applied is equivalent to a mass of 0.2 kg. In some embodiments,the pressure applied is equivalent to a mass of 0.3 kg. In someembodiments, the pressure applied is equivalent to a mass of 0.4 kg. Insome embodiments, the pressure applied is equivalent to a mass of 0.5kg. In some embodiments, the pressure applied is equivalent to a mass of0.6 kg. In some embodiments, the pressure applied is equivalent to amass of 0.7 kg. In some embodiments, the pressure applied is equivalentto a mass of 0.8 kg. In some embodiments, the pressure applied isequivalent to a mass of 0.9 kg. In some embodiments, the pressureapplied is equivalent to a mass of 1 kg. In some embodiments, thepressure applied is equivalent to a mass of 1.5 kg. In some embodiments,the pressure applied is equivalent to a mass of 2 kg. In someembodiments, the pressure applied is equivalent to a mass of 2.5 kg. Insome embodiments, the pressure applied is equivalent to a mass of 3 kg.In some embodiments, the pressure applied is equivalent to a mass of 3.5kg. In some embodiments, the pressure applied is equivalent to a mass of4 kg. In some embodiments, the pressure applied is equivalent to a massof 4.5 kg. In some embodiments, the pressure applied is equivalent to amass of 5 kg.

In some embodiments, the pressure is applied using a garment, such as abelt.

In some embodiments, the suitable skin-electrode impedance is between100 and 650 kΩ. In some embodiments, the suitable skin-electrodeimpedance is 602 kΩ. In some embodiments, the suitable skin-electrodeimpedance is less than 150 kΩ. In some embodiments, the suitableskin-electrode impedance is 227 kΩ. In some embodiments, the suitableskin-electrode impedance is 135 kΩ.

In some embodiments, the cutaneous contact is configured to haveskin-electrode impedance of less than 150 kΩ.

In some embodiments, the cutaneous contact is configured to haveskin-electrode impedance of between 5 to 150 kΩ. In some embodiments,the cutaneous contact is configured to have skin-electrode impedance ofbetween 10 to 150 kΩ. In some embodiments, the cutaneous contact isconfigured to have skin-electrode impedance of between 20 to 150 kΩ. Insome embodiments, the cutaneous contact is configured to haveskin-electrode impedance of between 30 to 150 kΩ. In some embodiments,the cutaneous contact is configured to have skin-electrode impedance ofbetween 40 to 150 kΩ. In some embodiments, the cutaneous contact isconfigured to have skin-electrode impedance of between 50 to 150 kΩ. Insome embodiments, the cutaneous contact is configured to haveskin-electrode impedance of between 60 to 150 kΩ. In some embodiments,the cutaneous contact is configured to have skin-electrode impedance ofbetween 70 to 150 kΩ. In some embodiments, the cutaneous contact isconfigured to have skin-electrode impedance of between 80 to 150 kΩ. Insome embodiments, the cutaneous contact is configured to haveskin-electrode impedance of between 90 to 150 kΩ. In some embodiments,the cutaneous contact is configured to have skin-electrode impedance ofbetween 100 to 150 kΩ. In some embodiments, the cutaneous contact isconfigured to have skin-electrode impedance of between 110 to 150 kΩ. Insome embodiments, the cutaneous contact is configured to haveskin-electrode impedance of between 120 to 150 kΩ. In some embodiments,the cutaneous contact is configured to have skin-electrode impedance ofbetween 130 to 150 kΩ. In some embodiments, the cutaneous contact isconfigured to have skin-electrode impedance of between 140 to 150 kΩ.

In some embodiments, the cutaneous contact is attached to an elastomericstructure that is configured to deform when placed on the abdomen of thepregnant human subject to create a skin-electrode impedance of less than150 kΩ.

In some embodiments, the cutaneous contact is attached to an elastomericstructure that is configured to deform when placed on the abdomen of thepregnant human subject to create a skin-electrode impedance of between 5to 150 kΩ. In some embodiments, the cutaneous contact is attached to anelastomeric structure that is configured to deform when placed on theabdomen of the pregnant human subject to create a skin-electrodeimpedance of between 10 to 150 kΩ. In some embodiments, the cutaneouscontact is attached to an elastomeric structure that is configured todeform when placed on the abdomen of the pregnant human subject tocreate a skin-electrode impedance of between 20 to 150 kΩ. In someembodiments, the cutaneous contact is attached to an elastomericstructure that is configured to deform when placed on the abdomen of thepregnant human subject to create a skin-electrode impedance of between30 to 150 kΩ. In some embodiments, the cutaneous contact is attached toan elastomeric structure that is configured to deform when placed on theabdomen of the pregnant human subject to create a skin-electrodeimpedance of between 40 to 150 kΩ. In some embodiments, the cutaneouscontact is attached to an elastomeric structure that is configured todeform when placed on the abdomen of the pregnant human subject tocreate a skin-electrode impedance of between 50 to 150 kΩ. In someembodiments, the cutaneous contact is attached to an elastomericstructure that is configured to deform when placed on the abdomen of thepregnant human subject to create a skin-electrode impedance of between60 to 150 kΩ. In some embodiments, the cutaneous contact is attached toan elastomeric structure that is configured to deform when placed on theabdomen of the pregnant human subject to create a skin-electrodeimpedance of between 70 to 150 kΩ. In some embodiments, the cutaneouscontact is attached to an elastomeric structure that is configured todeform when placed on the abdomen of the pregnant human subject tocreate a skin-electrode impedance of between 80 to 150 kΩ. In someembodiments, the cutaneous contact is attached to an elastomericstructure that is configured to deform when placed on the abdomen of thepregnant human subject to create a skin-electrode impedance of between90 to 150 kΩ. In some embodiments, the cutaneous contact is attached toan elastomeric structure that is configured to deform when placed on theabdomen of the pregnant human subject to create a skin-electrodeimpedance of between 100 to 150 kΩ. In some embodiments, the cutaneouscontact is attached to an elastomeric structure that is configured todeform when placed on the abdomen of the pregnant human subject tocreate a skin-electrode impedance of between 110 to 150 kΩ. In someembodiments, the cutaneous contact is attached to an elastomericstructure that is configured to deform when placed on the abdomen of thepregnant human subject to create a skin-electrode impedance of between120 to 150 kΩ. In some embodiments, the cutaneous contact is attached toan elastomeric structure that is configured to deform when placed on theabdomen of the pregnant human subject to create a skin-electrodeimpedance of between 130 to 150 kΩ. In some embodiments, the cutaneouscontact is attached to an elastomeric structure that is configured todeform when placed on the abdomen of the pregnant human subject tocreate a skin-electrode impedance of between 140 to 150 kΩ.

In some embodiments, the electrode is configured to have a surfaceresistance suitable for sensing fetal electrocardiogram signals from apregnant human subject. In some embodiments, the cutaneous contact isconfigured to have a surface resistance of less than 1 Ω/square. In someembodiments, the cutaneous contact is configured to have a surfaceresistance between 0.01 and 1 Ω/square.

In some embodiments, the cutaneous contact is configured to have asurface resistance of 0.01 Ω/square. In some embodiments, the cutaneouscontact is configured to have a surface resistance of 0.02 Ω/square. Insome embodiments, the cutaneous contact is configured to have a surfaceresistance of 0.03 Ω/square. In some embodiments, the cutaneous contactis configured to have a surface resistance of 0.04 Ω/square. In someembodiments, the cutaneous contact is configured to have a surfaceresistance of 0.05 Ω/square. In some embodiments, the cutaneous contactis configured to have a surface resistance of 0.06 Ω/square. In someembodiments, the cutaneous contact is configured to have a surfaceresistance of 0.07 Ω/square. In some embodiments, the cutaneous contactis configured to have a surface resistance of 0.08 Ω/square. In someembodiments, the cutaneous contact is configured to have a surfaceresistance of 0.09 Ω/square. In some embodiments, the cutaneous contactis configured to have a surface resistance of 0.1 Ω/square. In someembodiments, the cutaneous contact is configured to have a surfaceresistance of 0.2 Ω/square. In some embodiments, the cutaneous contactis configured to have a surface resistance of 0.3 Ω/square. In someembodiments, the cutaneous contact is configured to have a surfaceresistance of 0.4 Ω/square. In some embodiments, the cutaneous contactis configured to have a surface resistance of 0.5 Ω/square. In someembodiments, the cutaneous contact is configured to have a surfaceresistance of 0.6 Ω/square. In some embodiments, the cutaneous contactis configured to have a surface resistance of 0.7 Ω/square. In someembodiments, the cutaneous contact is configured to have a surfaceresistance of 0.8 Ω/square. In some embodiments, the cutaneous contactis configured to have a surface resistance of 0.9 Ω/square. In someembodiments, the cutaneous contact is configured to have a surfaceresistance of 1 Ω/square.

In some embodiments, the electrode is configured to have a capacitancesuitable for sensing fetal electrocardiogram signals from a pregnanthuman subject. In some embodiments, the capacitance is from 1 nF to 0.5μF. In some embodiments, the capacitance is 5 nF. In some embodiments,the capacitance is 10 nF. In some embodiments, the capacitance is 15 nF.In some embodiments, the capacitance is 20 nF. In some embodiments, thecapacitance is 25 nF. In some embodiments, the capacitance is 30 nF. Insome embodiments, the capacitance is 35 nF. In some embodiments, thecapacitance is 40 nF. In some embodiments, the capacitance is 45 nF. Insome embodiments, the capacitance is 50 nF. In some embodiments, thecapacitance is 60 nF. In some embodiments, the capacitance is 70 nF. Insome embodiments, the capacitance is 80 nF. In some embodiments, thecapacitance is 90 nF. In some embodiments, the capacitance is 80 nF. Insome embodiments, the capacitance is 0.1 μF. In some embodiments, thecapacitance is 80 nF. In some embodiments, the capacitance is 0.2 μF. Insome embodiments, the capacitance is 80 nF. In some embodiments, thecapacitance is 0.3 μF. In some embodiments, the capacitance is 80 nF. Insome embodiments, the capacitance is 0.4 μF. In some embodiments, thecapacitance is 80 nF. In some embodiments, the capacitance is 0.5 μF.

Without intending to be limited to any particular theory, thecapacitance of the electrodes increases as the surface area of thecutaneous contact that contacts the skin of the pregnant human subjectincreases. Additionally, without intending to be limited to anyparticular theory, the capacitance of the electrodes decreases as thepressure applied to the cutaneous contact increases.

In some embodiments, the electrode is configured to detect a fetalelectrocardiogram signal having a signal to noise ratio between −20 dBand 50 dB. In some embodiments, the electrode is configured to detect afetal electrocardiogram signal having a signal to noise ratio between 0dB and 50 dB. In some embodiments, the electrode is configured to detecta fetal electrocardiogram signal having a signal to noise ratio lessthan 50 dB.

The Cutaneous Contact

In some embodiments, the cutaneous contact is an electrically conductivefabric. Electrically conductive fabrics can be made with conductivefibers, such as, for example, metal strands woven into the constructionof the fabric. Examples of electrically conductive fabrics suitable foruse in electrodes according to some embodiments of the present inventioninclude, but are not limited to, the textile electrodes disclosed inSensors, 12 16907-16919, 2012. Another example of electricallyconductive fabrics suitable for use in electrodes according to someembodiments of the present invention include, but are not limited to,the textile electrodes disclosed in Sensors, 14 11957-11992, 2014.

The electrically conductive fabric may be stretchable. Alternatively,the electrically conductive fabric may not be stretchable. Theelectrically conductive fabric may be capable of stretching up to 50%,alternatively, 40%, alternatively, 30%, alternatively 20%, alternatively20%, alternatively, 10%, alternatively, 9%, alternatively, 8%,alternatively, 7%, alternatively, 6%, alternatively, 5%, alternatively,4%, alternatively, 3%, alternatively, 2%, alternatively, 1%.

In some embodiments, the electrically conductive fabric is anisotropic.In some embodiments, the anisotropy is from 50% to 100%. As used herein,the term anisotropy refers to the difference in resistance of theelectrically conductive fabric measured in the main direction, comparedto the direction perpendicular to the main direction. As used herein,the term “main direction refers to the direction that the fabric waswoven. In some embodiments, the anisotropy of the electricallyconductive fabric is configured to have an anisotropy suitable forsensing fetal electrocardiogram signals from a pregnant human subject.In some embodiments, the anisotropy is 62%.

In some embodiments, the electrically conductive fabric is configured tobe oriented so the current recorded is the electrical activity that isgenerated by the fetal and/or maternal heart, and flows along the maindirection of the fabric to the lead wire. In some embodiments, theelectrically conductive fabric is configured to be oriented so thecurrent recorded is the electrical activity that is generated by thefetal and/or maternal heart, and flows along the direction of the fabrichaving the least resistance to the lead wire.

In some embodiments, the conductivity of one side of the electricallyconductive fabric is greater than the other. In some embodiments, theside of the electrically conductive fabric with the greater conductivityforms cutaneous contact.

In some embodiments, the electrically conductive fabric has a thicknessbetween 0.3 and 0.5 mm. In some embodiments, the thickness of theelectrically conductive fabric is 0.3 mm. In some embodiments, thethickness of the electrically conductive fabric is 0.4 mm. In someembodiments, the thickness of the electrically conductive fabric is 0.5mm.

In some embodiments, the electrically conductive fabric is thesilver-based conductive fabric sold under the tradename ORANGE IT. Anexample of this electrically conductive fabric is shown in FIG. 5.

In some embodiments, the electrically conductive fabric is thesilver-based conductive fabric sold under the tradename C+, sold byClothing+, St. Petersburg, Fla., USA. An example of this electricallyconductive fabric is shown in FIG. 6.

In some embodiments, the electrically conductive fabric is thesilver-based conductive fabric sold under the tradename SHAOXING17, soldby Shaoxing Yunjia Textile Prodict Co. Ltd., Zhejiang, China. An exampleof this electrically conductive fabric is shown in FIG. 7.

In some embodiments, the electrically conductive fabric is thesilver-based conductive fabric sold under the tradename SHAOXING27, soldby Shaoxing Yunjia Textile Prodict Co. Ltd., Zhejiang, China. An exampleof this electrically conductive fabric is shown in FIG. 8.

In some embodiments, the electrically conductive fabric is thesilver-based conductive fabric sold under the tradename SHIELDEXTECHNIK-TEX P130-B, sold by Shieldex Trading USA, Palmyra, N.Y., USA. Anexample of this electrically conductive fabric is shown in FIG. 9.

In some embodiments, the electrically conductive fabric is thesilver-based conductive fabric sold under the tradename SILVER30, soldby Shaoxing Yunjia Textile Prodict Co. Ltd., Zhejiang, China. An exampleof this electrically conductive fabric is shown in FIG. 10.

Systems for Sensing Fetal Cardiac Electrical Activity

In some embodiments, the arrangement of the electrodes provides a systemfor recording, detecting and analyzing fetal cardiac electrical activitydata regardless of sensor position, fetal orientation, fetal movement,or gestational age. In some embodiments, the electrodes are attached, orpositioned, on the abdomen of the pregnant human subject in theconfiguration shown in FIG. 11. In some embodiments, the electrodes aredivided into channels comprising a pair of electrodes, and cardiacelectrical activity data is recorded simultaneously from the channels.In some embodiments, the channels output the acquired signal data,corresponding to the recorded cardiac electrical activity data.

Referring to FIG. 12, in some embodiments, the system for recording,detecting and analyzing fetal cardiac electrical activity comprises askin-electrode interface, at least one electrode, an analogpre-processing module, an analog to digital converter/microcontroller(ADC/MCU) module, a communications module, a smartphone module, and acloud computing module.

In some embodiments, the analog pre-processing module performs at leastone function selected from the group consisting of: amplification of therecorded signals, and filtering the recorded signals.

In some embodiments, the ADC/MCU module performs at least one taskselected from the group consisting of: converting analog signals todigital signals, converting the recorded signals to digital signals,compressing the data, digital filtering, and transferring the recordedelectrocardiogram signals data to the transmitter.

In some embodiments, the communications module transmits the recordedsignals to a wireless receiver.

In some embodiments, the system for recording, detecting and analyzingfetal cardiac electrical activity data regardless of sensor position,fetal orientation, fetal movement, or gestational age is the systemdisclosed in International Patent Application Serial No.PCT/IL2015/050407.

In some embodiments, at least one electrode pair is used to obtain theacquired signal data. In some embodiments, For example, by way of anon-limiting illustration, in some embodiments, the channels arespecified as follows:

1. B1-B3

2. B1-B2

3. B2-B3

4. A1-A4

5. A2-A3

6. A2-A4

In some embodiments, the signal data corresponding to fetal cardiacelectrical activity data are extracted from the acquired signal data.

In some embodiments, the signal data corresponding to fetal cardiacelectrical activity data are extracted from the acquired signal dataaccording to the methods described in U.S. patent application Ser. No.14/921,489.

In one embodiment, the present invention provides a garment, comprising:

at least one pair of electrodes,

-   -   wherein the at least one pair of electrodes are configured, when        the garment is worn by the pregnant human subject, such that the        individual electrodes of the at least one electrode pair        encircle the uterus of the pregnant human subject, and    -   wherein the individual electrodes of the at least one electrode        pair comprise:        -   a) a cutaneous contact for sensing fetal electrocardiogram            signals from a pregnant human subject;        -   b) a connector in electrical contact with the cutaneous            contact for connection to a lead wire; and        -   c) a substructure for attachment to a human pregnant subject            -   wherein, the cutaneous contact is configured on the                substructure to allow a surface of the cutaneous contact                to be in electrical communication with the skin of the                pregnant human subject;    -   wherein cardiac electrical activity data is recorded from the at        least one sensor pair.

Referring to FIG. 13, an example of a garment according to someembodiments of the present invention is shown. In the embodiment shown,6 electrodes are incorporated into a belt, wherein the belt, when worn,positions the electrodes on the abdomen of the pregnant mother, suchthat the electrodes contact the skin of the abdomen of the pregnantmother, and the electrodes are positioned in a circumferentialarrangement around the uterus. In the embodiments shown, the belt alsocontains additional sensors and a transmitter.

In some embodiments, the additional sensors are acoustic sensors.

Reference is now made to the following examples, which together with theabove descriptions illustrate some embodiments of the invention in anon-limiting fashion.

EXAMPLES Example 1: Electrodes According to Some Embodiments of thePresent Invention

Various electrodes were manufactured according to the embodiment shownin FIG. 1 and evaluated. The following parameters were tested: thesurface resistance/resistivity (MSSR); basic transfer function testing(BTFT); bio-parameters (PhysioPM); and real-life recordings of fetalcardiac electrical signals (RLPysioPM). Table 1 summarizes theelectrodes tested.

TABLE 1 Measured* Surface Surface Available conductivity conductivitysize Serial# ID [Ohm/Sq] [Ohm/Sq] [cm × cm] Materials Notes 1 Orange_IT<2 3.5 20*20 Silver Anisotropic, Stechable 2 C+ <4 4 70*70 SilverAnisotropic, Stechable 3 Shaoxing17 — 0.3 1 m{circumflex over ( )}2Silver Isotropic, Non-strechable 4 Shaoxing27 — 0.6 1 m{circumflex over( )}2 Silver Isotropic, Non-strechable 5 Tech P130 + B <5 1.1 40*40Silver Isotropic, Strechable 6 Silver30 — 3.5 20*15 Silver Isotropic,Strechable

FIG. 5 shows a micrograph of electrically conductive fabric usedelectrode serial no. 1. FIG. 6 shows a micrograph of electricallyconductive fabric used electrode serial no. 2. FIG. 7 shows a micrographof electrically conductive fabric used electrode serial no. 3. FIG. 8shows a micrograph of electrically conductive fabric used electrodeserial no. 4. FIG. 9 shows a micrograph of electrically conductivefabric used electrode serial no. 5. FIG. 10 shows a micrograph ofelectrically conductive fabric used electrode serial no. 6.

Table 2 a-f shows the MSSR values observed from the electrodes tested.Table 3 shows the observed anisotropy of the electrodes tested.

TABLE 2a Sens 1 AVG Aniso- Inject Measure Check? M1 M2 M3 [Ω] tropicNotes AB CD 1 0.243 0.245 0.246 0.245 0.230 CD AB 1 0.228 0.227 0.2260.227 BA DC 1 0.224 0.225 0.222 0.224 DC BA 1 0.227 0.224 0.222 0.224 BCDA 1 0.489 0.487 0.484 0.487 0.459 DA BC 0 0 0 0 0.000 CB AD 1 0.4440.443 0.441 0.443 AD CB 1 0.45 0.448 0.446 0.448

TABLE 2b Sens 2 AVG Aniso- Inject Measure Check? M1 M2 M3 [Ω] tropicNotes AB CD 1 1.022 1.02 1.014 1.019 1.032 CD AB 1 0.999 0.996 0.9950.997 BA DC 1 0.994 0.984 0.979 0.986 DC BA 1 1.13 1.123 1.123 1.125 BCDA 0 0 0 0 0.000 NaN Main DA BC 0 0 0 0 0.000 direc- CB AD 0 0 0 0 0.000tion AD CB 0 0 0 0 0.000

TABLE 2c Sens 3 AVG Iso- Inject Measure Check? M1 M2 M3 [Ω] tropic NotesAB CD 1 0.039 0.038 0.04 0.039 0.031 CD AB 1 0.027 0.024 0.025 0.025 BADC 1 0.023 0.023 0.023 0.023 DC BA 1 0.036 0.035 0.035 0.035 BC DA 10.026 0.028 0.026 0.027 0.026 DA BC 1 0.024 0.025 0.023 0.024 CB AD 10.027 0.026 0.026 0.026 AD CB 1 0.027 0.024 0.026 0.026

TABLE 2d Sens 4 AVG Iso- Inject Measure Check? M1 M2 M3 [Ω] tropic NotesAB CD 1 0.026 0.063 0.064 0.051 0.058 CD AB 1 0.058 0.057 0.059 0.058 BADC 1 0.06 0.059 0.058 0.059 DC BA 1 0.066 0.065 0.066 0.066 BC DA 10.045 0.045 0.045 0.045 0.044 DA BC 1 0.043 0.044 0.043 0.043 CB AD 10.045 0.043 0.043 0.044 AD CB 1 0.044 0.042 0.043 0.043

TABLE 2e Sens 5 AVG Aniso- Inject Measure Check? M1 M2 M3 [Ω] tropicNotes AB CD 1 0.222 0.224 0.223 0.223 0.194 CD AB 1 0.212 0.211 0.2130.212 BA DC 1 0.22 0.219 0.222 0.220 DC BA 1 0.233 0.065 0.066 0.121 BCDA 1 0.074 0.073 0.073 0.073 0.075 DA BC 1 0.083 0.084 0.084 0.084 CB AD1 0.074 0.075 0.075 0.075 AD CB 1 0.065 0.067 0.067 0.066

TABLE 2f Sens 6 AVG Aniso- Inject Measure Check? M1 M2 M3 [Ω] tropicNotes AB CD 1 0.05 0.048 0.049 0.049 0.046 CD AB 1 0.038 0.039 0.0370.038 BA DC 1 0.055 0.057 0.056 0.056 DC BA 1 0.043 0.041 0.042 0.042 BCDA 1 0.911 0.903 0.898 0.904 0.898 DA BC 1 0.904 0.891 0.897 0.897 CB AD1 0.885 0.886 0.882 0.884 AD CB 1 0.903 0.903 0.908 0.905

TABLE 3 ID Main direction 2nd direction Anisotropy 1 0.230 0.459 50% 20.000* 1.032 100%  3 0.026 0.031 16% 4 0.044 0.058 25% 5 0.075 0.194 62%6 0.046 0.898 95%

The impedance between the fabric and the lead connector was alsodetermined. The electrodes were connected to a copper sheet, and apressure of 34.386 kPa was applied, using a 1.01026 kg weight. Themeasured impedance of the measuring system was 0.109Ω, and this valuewas subtracted from the measured impedance of the electrodes. Theresults are shown in Table 4. Electrode serial no. 5 was observed tohave the greatest surface area in contact with the surface.

TABLE 4 AVG Value ID Check? M1 M2 M3 [Ω] [Ω] 1 1 0.694 0.685 0.682 0.6870.578 2 1 0.461 0.460 0.452 0.458 0.349 3 1 0.206 0.205 0.206 0.2060.097 4 1 0.271 0.269 0.268 0.269 0.160 5 1 0.309 0.307 0.308 0.3080.199 6 1 0.709 0.662 0.664 0.678 0.569

Electrodes 3-5 performed best. Performance was scored as follows:

Req. Test ID Category Category Details 0.1 Performance General RecordECG signals 1.1 Performance MSRR Surface resistivity below 1 [Ω · m] 1.2Performance MSRR Surface resistance below 1 [Ω/sq] 2.1 Performance BTFTSINAD is higher than 50 dB 2.2 Performance BTFT SNR is higher than 50 dB2.3 Performance BTFT CORR COEF higher than 0.95 3.1 Performance PysioPMSkin-Sensor impedance below 0.15 [MΩ] 3.2 Performance PysioPM Self-noiseof the sensor below 0.1 μV 3.3 Performance PysioPM Immunity to motionartifacts 3.4 Performance PysioPM Power-line noise rejection higher than80 dB 4.1 Performance RLPysioPM Fetal ECG is visible in more than 1record 4.2 Performance RLPysioPM Fetal ECG SNR is higher than 1 dB 3.5Performance RLPysioPM Relative fetal ECG SNR (relative to the referencesensor) is higher than 0.85

A summary of the MSSR results for electrodes 3-5 is shown in Table 5.The fabric of electrode serial no. 6 was weak, and has large voidsbetween the fibers (see FIG. 10) and was therefore unsuitable. Electrodeserial no. 2 was excluded because the surface resistivity was greaterthan 1 Ω/square.

TABLE 5 Surface resistance Main 2nd Aniso- ID direction direction tropyS2C Notes 3 0.026 0.031 0.163 0.097 Lowest resistance, non- stretchable,Isotropic 4 0.044 0.058 0.251 0.160 Mid 5 0.075 0.194 0.616 0.199 Lowresistance, Highest Anisotropy, highly stretchable

BTFT Results: BTFT measurements were obtained using the methodsdescribed in Example 3 below. Table 6 shows the results.

TABLE 6 Relative diff SINAD SNR ID CORRCOEF CORRLAG RMS [%] Input OutputRel RelRef Input Output Rel Ref 1 0 0.012 48.545 48.541 0.008% 0.000%53.852 53.836 0.029% 1 1 0 0.010 47.964 47.956 0.015% 1.205% 54.27854.242 0.066% 2 1 0 0.016 48.088 48.077 0.021% 0.955% 54.173 54.1360.068% 3 1 0 0.010 48.231 48.222 0.018% 0.657% 54.197 54.161 0.067% 4 10 0.015 48.303 48.293 0.020% 0.511% 54.042 54.006 0.066% 5 1 0 0.01548.527 48.517 0.020% 0.049% 54.137 54.102 0.064% 6 1 0 0.014 48.60648.597 0.018% 0.115% 54.113 54.073 0.074%

CORRCOEF: is the linear correlation coefficient between the input andthe output signals; CORRLAG: is the lag between the input and outputsignals; Relative diff RMS: is the relative difference in the RMS of theinput and output signals in %; SINAD.Rel: is the relative percentagedifference in the SINAD values between the input and the output signals;SINAD.RelRef: is the relative percentage difference in the signal tonoise and distortion ratio (SINAD) values between the output signal andthe reference signal; SNR.Rel: is the relative percentage difference inthe SNR values between the input and the output signals. The BTFTresults show that the electrodes that have the best performance in termsof SNR and relative SINAD is electrode serial no. 5 followed byelectrode serial no. 4, then electrode serial no. 3.

PysioPM: PysioPM measurements were obtained according to the methodsdescribed in Example 4. Table 7 shows the results of the measuredimpedance.

TABLE 7 ID Sens1 Sens2 Sens3 Sens4 MAXDIFF 3 0.733 0.667 0.651 0.75413.66% 4 1.396 1.495 1.281 1.503 14.77% 5 4.251 3.1 3.551 3.921 27.08%

The values observed include the resistance of a 5 cm lead wire, thecopper sheet, and a cable connected to the copper sheet.

Impedance of the Interface Between the Electrode and the Skin: Theimpedance was measured between 2 electrodes placed on skin 20 mm apart.Table 8 shows the average of 3 experiments.

TABLE 8 ID Average Bioimpedance [MΩ] 3 0.602 4 0.227 5 0.135

Recorded ECG Signals Data Using the Electrodes: FIG. 14, panels a-c showrecorded ECG signals data using electrode serial nos. 3-5 respectively.Electrodes 3-5 were able to filter out powerline noise, and had similaramplitudes. However, all electrodes were susceptible to movementartifacts.

ECG signal were recorded from two pregnant subjects at week 25 and week28, using either electrodes 3, 4, 5, and a comparison electrode, using awet contact electrode, using the electrode position B1-B3 (see FIG. 11for the electrode position). FIG. 15, panels a-d, and FIG. 16, panelsa-d show the recorded ECG signals data using electrode serial nos. 3-5,and the GE comparison electrode respectively at 25 weeks in the twosubjects. Fetal ECG were visible in the traces.

Example 2: Measuring Surface Resistivity and Resistance

FIG. 17 shows an experimental set up to determine surface resistivityand resistance of an electrically conductive fabric according to someembodiments of the present invention. A, B, C, and D are point contactconnectors. To measure surface resistivity, current was introduced andrecorded according to the following protocol:

1. Connect the sample as described in the background section.

2. Make sure that the current source is running and stable.

3. Inject AB, measure CD;

4. Inject CD, measure AB;

5. Inject BA, measure DC;

6. Inject DC, measure BA;

7. Inject BC, measure DA;

8. Inject DA, measure BC;

9. Inject CB, measure AD;

10. Inject AD, measure CB;

Surface resistance was calculated according to the following:

${{\exp ( {- \frac{\pi \; R_{{AB},{CD}}}{R_{s}}} )} + {\exp ( {- \frac{\pi \; R_{{BC},{AD}}}{R_{s}}} )}} = {1{\mspace{11mu} \;}{where}}$${RAB},{{{CD}\lbrack\Omega\rbrack} = {\frac{V_{DC}}{i_{AB}} = {\frac{V_{D}}{i_{AB}} = \frac{V_{D} - V_{C}}{i_{AB}}}}}$

is the resistance measured between C and D while introducing currentbetween points A and B; and i_(AB) [A] is the injected current betweenpoints A and B; and d [m] is the thickness of the sample; and ρ is theresistivity.

ρ = R_(s)d[Ω] ⋅ m $R_{s} = {\frac{\pi}{\ln \; 2} \cdot R}$R = R_(vertical) = R_(horizontal)$R_{vertical} = ( \frac{R_{{BC},{CD}} + R_{{CD},{AB}} + R_{{BA},{DC}} + R_{{DC},{BA}}}{2} )$$R_{horizontal} = ( \frac{R_{{BC},{DA}} + R_{{DA},{BC}} + R_{{CB},{AD}} + R_{{AD},{CB}}}{2} )$

The above protocol was performed using an electrode alone, or anelectrode contacting a copper sheet (to measure the resistivity of theelectrode-surface interface). Additionally, measurements were obtainedafter the electrically conductive fabric was stretched either 20%, or50% in the man direction, or in the direction perpendicular to the maindirection.

Example 3: Basic Transfer Function Testing

An electrode was placed on a copper sheet, such that the cutaneouscontact is in contact with the copper sheet, and a 1 kg mass was appliedto the electrode. The copper sheet was connected to the positiveterminal of a signal generator, the electrode was connected to thepositive input of an amplifier, and the other input of the amplifier wasconnected to ground. FIG. 18 shows the experimental setup describedabove. A 30 Hz signal was generated by the signal amplifier, and thefollowing parameters were recorded:

1. Time domain:

-   -   a. amplitude-2-amplitude; and    -   b. non-zero division; and    -   c. time shifts; and    -   d. cross correlation; and    -   e. correlation coefficient; and    -   f. Histogram: Mean, RMS, STD.

2. Frequency domain: a. Welch PSD estimation (magnitude); and

-   -   b. Cross coherence; and    -   c. Main frequency magnitude; and    -   d. Dominant frequencies magnitude; and    -   e. SINAD, SNR.

Example 4: Electrophysiological Performance Measurements

The source of the physiological signals detected using the electrodesaccording to some embodiments of the present invention are locatedwithin the body of the pregnant human subject and have extremely lowamplitude and low frequency. Without intending to be limited by anyparticular theory, the physiological signals flow within the body of thepregnant human subject by the movement of ions. The electrodes accordingto some embodiments of the present invention act as signal transducers,and transduce the movement of ions to the movements of electrons. Theskin-electrode interface (SSI) is one determining factor of theelectrode's ability to transduce the physiological signals.

The SSI for the electrodes according to some embodiments of the presentinvention may be modeled by a parallel circuit of an ohmic andcapacitive impedance with an additional Warburg resistance (see FIG.19). Without intending to be limited to any particular theory, both theconductive and the capacitive compartments affect the performance of anelectrode according to some embodiments of the present invention. Theskin-electrode impedance (SSiM) is equivalent to the impedance of thecircuit shown in FIG. 19, and ranges from 10 kΩ to 100 MΩ. Decreasingthe impedance improves the performance of an electrode according to someembodiments of the present invention. Decreasing impedance may beachieved by increasing the surface areas of the cutaneous contact, or byreducing the resistivity of the cutaneous contact. An increase in inputimpedance and a decrease in input capacitance of the amplifier may alsoimproves the performance of an electrode according to some embodimentsof the present invention.

In the test protocol, electrodes were applied to the skin of a subject'shand, according to the arrangement shown in FIG. 20. The surface of thehand having first been cleaned. Four VELCRO straps were applied, thepressure of the straps was confirmed to be equal, using a surfacepressure sensor. Test electrodes were then inserted under the straps.The pressure that the electrodes contact the skin was confirmed to beequal, using a surface pressure sensor. Impedance was measured asfollows:

-   -   2-wire: measure the 2wire resistance between the S_(i)        electrodes and the S_(o) electrodes (2 measurements).    -   4-wire: use the S_(i) electrodes as the injectors and the S_(o)        electrodes as the measurers. Measure the resistance (1        measurement).    -   Capacitance measurement: measure the 2wire capacitance between        the S_(i) electrodes and the S_(o) electrodes (2 measurements).

A 150 mV_(pp) sine wave was applied to the S_(i) electrodes, and thevoltage developed at the S_(o) electrodes was recorded using a BioPacamplifier, sold by BioPac systems Inc. Recordings were obtained using asine wave of the following frequencies: 0.1, 1, 5, 10, 15, 20, 25, 30,35, 40, 45, 50, 55, 60, 70, 80, 90,

Publications cited throughout this document are hereby incorporated byreference in their entirety. Although the various aspects of theinvention have been illustrated above by reference to examples andpreferred embodiments, it will be appreciated that the scope of theinvention is defined not by the foregoing description but by thefollowing claims properly construed under principles of patent law.

What is claimed is:
 1. An electrode, wherein electrode is configured todetect fetal electrocardiogram signals wherein the electrode comprises:a. a cutaneous contact for sensing fetal electrocardiogram signals froma pregnant human subject; b. a connector in electrical contact with thecutaneous contact for connection to a lead wire; and c. a substructurefor attachment to a human pregnant subject, wherein, the cutaneouscontact is configured on the substructure to allow a surface of thecutaneous contact to be in electrical communication with the skin of thepregnant human subject.
 2. The electrode of claim 1, wherein thecutaneous contact is configured to have skin-electrode impedance ofgreater than 150 kΩ.
 3. The electrode of claim 1, wherein the cutaneouscontact is configured to have skin-electrode impedance of less than 150kΩ.
 4. The electrode of claim 1, wherein the cutaneous contact isconfigured to have skin-electrode impedance of between 5 to 150 kΩ. 5.The electrode of claim 1, wherein the cutaneous contact is attached toan elastomeric structure that is configured to deform when placed on theabdomen of the pregnant human subject to create a skin-electrodeimpedance of less than 150 kΩ.
 6. The electrode of claim 1, wherein thecutaneous contact is attached to an elastomeric structure that isconfigured to deform when placed on the abdomen of the pregnant humansubject to create a skin-electrode impedance of between 5 to 150 kΩ. 7.The electrode of claim 1, wherein the cutaneous contact is configured tohave a surface resistance of less than 1 Ω/square.
 8. The electrode ofclaim 1, wherein the cutaneous contact is configured to have a surfaceresistance between 0.01 and 1 Ω/square.
 9. The electrode of claim 1,wherein the signal to noise ratio of the fetal electrocardiogram signalsis between −20 dB and 50 dB.
 10. The electrode of claim 1, wherein thesignal to noise ratio of the fetal electrocardiogram signals is between0 dB and 50 dB.
 11. The electrode of claim 1, wherein the cutaneouscontact is an electrically conductive fabric.
 12. The electrode of claim11, wherein the electrically conductive fabric has a skin-electrodeimpedance of less than 150 kΩ.
 13. The electrode of claim 11, whereinthe electrically conductive fabric has a skin-electrode impedance ofbetween 5 to 150 kΩ.
 14. The electrode of claim 11, wherein the surfaceof the electrically conductive fabric that forms the cutaneous contactis configured to have a surface resistance of less than 1 Ω/square. 15.A garment, comprising: a. at least one pair of electrodes, wherein theat least one pair of electrodes are configured, when the garment is wornby the pregnant human subject, such that the individual electrodes ofthe at least one electrode pair encircle the uterus of the pregnanthuman subject, and wherein the individual electrodes of the at least oneelectrode pair comprise:
 1. a cutaneous contact for sensing fetalelectrocardiogram signals from a pregnant human subject;
 2. a connectorin electrical contact with the cutaneous contact for connection to alead wire; and
 3. a substructure for attachment to a human pregnantsubject, wherein, the cutaneous contact is configured on thesubstructure to allow a surface of the cutaneous contact to be inelectrical communication with the skin of the pregnant human subject;wherein cardiac electrical activity data is recorded from the at leastone sensor pair.